HCS Roll-On Antiperspirant

Manufacturer: Dyad Medical Sourcing, LLC
Effective date: 2022-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:49:23

Label at a glance#

ProductHCS Roll-On Antiperspirant

Active ingredientAluminum Chlorohydrate

Label structure8 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 4.5%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm perspiration.

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed get medical help and contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Paraffinum Liquidum, Cetearyl Alcohol, Ceteareth-24, Isopropyl Palmitate, Magnesium Aluminum Silicate, Methylparaben, Propylparaben, Sodium Benzoate, Fragrance

Principal Display Panel – 96 each

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HCS

Model No.: HCS0069

Description: Roll-On Antiperspirant/

Deodorant, 1.5 oz.

Quantity: 1 Case (96 each)

Lot No.:

Manufacture Date:

Expiration Date:

Manufactured for:

Dyad Medical Sourcing, LLC

Bannockburn, IL 60015 • USA

MADE IN MALAYSIA

NDC 53175-004-01

Principal Display Panel – 1 Bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HCS

NDC 53175-004-01

Clean Fresh Scent
Roll-On
Antiperspirant/
Deodorant

Fights Wetness & Odor

1.5 FL. OZ. (44ml)

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53175-004-01	2024-01-30	C162847	48780-1	1030e365-53e9-111a-e063-dadaa90a10e2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53175-004-01	HCS Roll-On Antiperspirant	44 mL in 1 BOTTLE, DISPENSING	LIQUID	44		1
53175-004-01	HCS Roll-On Antiperspirant	96 in 1 CASE	LIQUID	96		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53175-004	HCS ROLL-ON ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LIQUID [DYAD MEDICAL SOURCING, LLC]	1	Legacy NDC, 2 package rows	20220429_78e65078-f0b1-487d-a5ae-3b7f39dd4d78.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

HCS Roll-On Antiperspirant
Aluminum Chlorohydrate
Water
Mineral Oil
Cetostearyl Alcohol
Isopropyl Palmitate
Magnesium Aluminum Silicate
Methylparaben
Propylparaben
Sodium Benzoate

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53175-004	53175-004-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Aluminum Chlorohydrate	HPN8MZW13M	ACTIB
Water	059QF0KO0R	IACT
Mineral Oil	T5L8T28FGP	IACT
Cetostearyl Alcohol	2DMT128M1S	IACT
Isopropyl Palmitate	8CRQ2TH63M	IACT
Magnesium Aluminum Silicate	6M3P64V0NC	IACT
Methylparaben	A2I8C7HI9T	IACT
Propylparaben	Z8IX2SC1OH	IACT
Sodium Benzoate	OJ245FE5EU	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c682b9cd-8d91-4410-b03d-4e746b440ff2			78e65078-f0b1-487d-a5ae-3b7f39dd4d78	2022-04-13	Warnings	Exact identifier spl id: c682b9cd-8d91-4410-b03d-4e746b440ff2 spl set id: 78e65078-f0b1-487d-a5ae-3b7f39dd4d78

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.